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Chapter 14 - Magnetic resonance spectroscopy in stroke

from Section 2 - Cerebrovascular disease

Published online by Cambridge University Press:  05 March 2013

Jonathan H. Gillard
Affiliation:
University of Cambridge
Adam D. Waldman
Affiliation:
Imperial College London
Peter B. Barker
Affiliation:
The Johns Hopkins University School of Medicine
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Summary

Introduction

As discussed in the previous chapter, a stroke is the rapidly developing loss of brain functions owing to a disturbance in the vessels supplying blood to the brain. This can be caused by ischemia (lack of blood supply) following thrombosis or embolism, or a hemorrhage. Acute stroke is a medical emergency, and imaging plays an important role in confirming (or otherwise) the clinical diagnosis of stroke, categorizing it as either ischemic or hemorrhagic, and identifying the underlying cause. Increasingly, imaging is also being used to guide therapeutic interventions and monitor their success. While traditionally X-ray computed tomography (CT) has been the imaging modality of choice (primarily because of its speed and widespread availability), MRI has been increasingly used because of its excellent contrast, high sensitivity and possibilities for multimodal acquisition (e.g., diffusion, perfusion, MR angiography, etc.). These topics are discussed in the following chapters.

Proton magnetic resonance spectroscopy (MRS) of the human brain was first demonstrated in the mid 1980s,[1–4] and shortly thereafter the first reports of its application to the study of human stroke appeared.[5,6] Although there have been reports of 31P,[7] 23Na,[8] and 13C [9] spectroscopy in human stroke, the majority of studies to date have utilized the proton nucleus, both because of its high sensitivity and the fact that proton MRS can be readily combined with conventional MRI without hardware modifications. Although the proton MRS studies performed in the early 1990s appeared to offer promise for diagnostic value in acute stroke, this modality has had relatively little impact for several reasons. The most important reason is the technical difficulty of performing it in a timely fashion in this patient population; secondly, much of the required clinical information is available from other (easier to perform) sequences, such as diffusion-weighted imaging (DWI), perfusion-weighted imaging (PWI), and T2-weighted MRI. Nevertheless, it is important to be aware of the spectroscopic correlates of acute and chronic infarction as, on occasion, MRS may be helpful in these clinical contexts.

Type
Chapter
Information
Clinical MR Neuroimaging
Physiological and Functional Techniques
, pp. 173 - 183
Publisher: Cambridge University Press
Print publication year: 2009

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References

Bottomley, PA, Edelstein, WA, Foster, TH, Adams, WA.In vivo solvent-suppressed localized hydrogen nuclear magnetic resonance spectroscopy: a window to metabolism?Proc Natl Acad Sci U S A. 1985; 82: 2148–2152.CrossRefGoogle ScholarPubMed
Luyten, PR, den Hollander, JA. Observation of metabolites in the human brain by MR spectroscopy. Radiology. 1986; 161: 795–798.CrossRefGoogle ScholarPubMed
Hanstock, CC, Rothman, DL, Prichard, JW, Jue, T, Shulman, RG. Spatially localized 1H NMR spectra of metabolites in the human brain. Proc Natl Acad Sci USA 1988; 85: 1821–1825.CrossRefGoogle ScholarPubMed
Frahm, J, Bruhn, H, Gyngell, ML, et al. Localized high-resolution proton NMR spectroscopy using stimulated echoes: initial applications to human brain in vivo. Magn Reson Med 1989; 9: 79–93.CrossRefGoogle ScholarPubMed
Berkelbach van der Sprenkel, JW, Luyten, PR, van Rijen, PC, Tulleken, CA, den Hollander, JA. Cerebral lactate detected by regional proton magnetic resonance spectroscopy in a patient with cerebral infarction. Stroke. 1988; 19: 1556–1560.CrossRefGoogle Scholar
Bruhn, H, Frahm, J, Gyngell, ML, et al. Cerebral metabolism in man after acute stroke: new observations using localized proton NMR spectroscopy. Magn Reson Med 1989; 9: 126–131.CrossRefGoogle ScholarPubMed
Helpern, JA, van de Linde, AMQ, Welch, KMA, et al. Acute elevation and recovery of intracellular [Mg2+] following human focal cerebral ischemia. Neurology 1993; 43: 1577–1581.CrossRefGoogle ScholarPubMed
Thulborn, KR, Gindin, TS, Davis, D, Erb, P. Comprehensive MR imaging protocol for stroke management: tissue sodium concentration as a measure of tissue viability in nonhuman primate studies and in clinical studies. Radiology 1999; 213: 156–166.CrossRefGoogle ScholarPubMed
Rothman, DL, Howseman, AM, Graham, GD, et al. Localized proton NMR observation of [3-13C]lactate in stroke after [1-13C]glucose infusion. Magn Reson Med 1991; 21: 302–307.CrossRefGoogle Scholar
Higuchi, T, Graham, SH, Fernandez, EJ, et al. Effects of severe global ischemia on N-acetylaspartate and other metabolites in the rat brain. Magn Reson Med 1997; 37: 851–857.CrossRefGoogle ScholarPubMed
Monsein, LH, Mathews, VP, Barker, PB, et al. Irreversible regional cerebral ischemia: serial MR imaging and proton MR spectroscopy in a nonhuman primate model. AJNR Am J Neuroradiol 1993; 14: 963– 70.Google Scholar
Sager, TN, Laursen, H, Fink-Jensen, A, et al. N-Acetylaspartate distribution in rat brain striatum during acute brain ischemia. J Cereb Blood Flow Metab 1999; 19: 164–172.CrossRefGoogle ScholarPubMed
Sager, TN, Laursen, H, Hansen, AJ. Changes in N-acetyl-aspartate content during focal and global brain ischemia of the rat. J Cereb Blood Flow Metab 1995; 15: 639–646.CrossRefGoogle ScholarPubMed
Higuchi, T, Fernandez, EJ, Maudsley, AA, et al. Mapping of lactate and N-acetyl-L-aspartate predicts infarction during acute focal ischemia: in vivo 1H magnetic resonance spectroscopy in rats. Neurosurgery 1996; 38: 121–129; discussion 9–30.CrossRefGoogle ScholarPubMed
van Zijl, PCM, Moonen, CTW. In situ changes in purine nucleotide, and N-acetyl concentrations upon inducing global ischemia in cat brain. Magn Reson Med 1993; 29: 381–385.CrossRefGoogle ScholarPubMed
Gillard, JH, Barker, PB, van Zijl, PCM, Bryan, RN, Oppenheimer, SM. Proton MR spectroscopic imaging in acute middle cerebral artery stroke. AJNR Am J Neuroradiol 1996; 17: 873–886.Google ScholarPubMed
Mathews, VP, Barker, PB, Blackband, SJ, Chatham, JC, Bryan, RN. Cerebral metabolites in patients with acute and subacute strokes: concentrations determined by quantitative proton MR spectroscopy. Am J Radiol 1995; 165: 633–638.Google ScholarPubMed
Munoz Maniega, S, Cvoro, V, Armitage, PA, et al. Choline and creatine are not reliable denominators for calculating metabolite ratios in acute ischemic stroke. Stroke 2008; 39: 2467–2469.CrossRefGoogle Scholar
Barker, P, Breiter, S, Soher, B, et al. Quantitative proton spectroscopy of canine brain: in vivo and in vitro correlations. Magn Reson Med 1994; 32: 157–163.CrossRefGoogle ScholarPubMed
Barker, PB, Gillard, JH, van Zijl, PCM, et al. Acute stroke: evaluation with serial proton magnetic resonance spectroscopic imaging. Radiology 1994; 192: 723–732.CrossRefGoogle Scholar
Duijn, JH,Matson, GB, Maudsley, AA, Hugg, JW, Weiner, MW.Human brain infarction: proton MR spectroscopy. Radiology 1992; 183: 711–718.CrossRefGoogle ScholarPubMed
Rehncrona, S, Rosen, I, Siesjo, BK.Brain lactic acidosis and ischemic cell damage: 1. biochemistry and neurophysiology. J Cereb Blood Flow Metab 1981; 1: 297–311.CrossRefGoogle ScholarPubMed
Petroff, OA, Graham, GD, Blamire, AM, et al. Spectroscopic imaging of stroke in humans: histopathology correlates of spectral changes. Neurology 1992; 42: 1349–1354.CrossRefGoogle ScholarPubMed
Alger, JR, Frank, JA, Bizzi, A, et al. Metabolism of human gliomas: assessment with H-1 MR spectroscopy and F-18 fluorodeoxyglucose PET. [See comments]Radiology 1990; 177: 633–641.CrossRefGoogle Scholar
Mathews, PM, Andermann, F, Silver, K, Karpati, G, Arnold, DL. Proton MR spectroscopic characterization of differences in regional brain metabolic abnormalities in mitochondrial encephalomyopathies. Neurology. 1993; 43: 2484–2490.CrossRefGoogle ScholarPubMed
Kruse, B, Barker, PB, van Zijl PC, M, et al. Multislice proton MR spectroscopic imaging in X-linked adrenoleukodystrophy. Ann Neurol 1994; 36: 595–608.CrossRefGoogle Scholar
Behar, KL, Rothman, DL, Spencer, DD, Petroff, OA. Analysis of macromolecule resonances in 1H NMR spectra of human brain. Magn Reson Med 1994; 32: 294–302.CrossRefGoogle ScholarPubMed
Saunders, DE, Howe, FA, van den Boogart, A, et al. Continuing ischemic damage after acute middle cerebral artery infarction in humans demonstrated by short-echo time proton spectroscopy. Stroke 1995; 26: 1007–1013.CrossRefGoogle Scholar
Hwang, JH, Graham, GD, Behar, KL, et al. Short echo time proton magnetic resonance spectroscopic imaging of macromolecule and metabolite signal intensities in the human brain. Magn Reson Med 1996; 35: 633–639.CrossRefGoogle ScholarPubMed
Saunders, DE, Howe, FA, van den Boogaart, A, Griffiths, JR, Brown, MM. Discrimination of metabolite from lipid and macromolecule resonances in cerebral infarction in humans using short echo proton spectroscopy. J Magn Reson Imaging. 1997; 7: 1116–1121.CrossRefGoogle ScholarPubMed
Hossman, K-A. Viability thresholds and the penumbra of focal ischemia. Ann Neurol 1994; 36: 557–565.CrossRefGoogle Scholar
Crockard, HA, Gadian, DG, Frackowiak, RS, et al. Acute cerebral ischaemia: concurrent changes in cerebral blood flow, energy metabolites, pH, and lactate measured with hydrogen clearance and 31P and 1H nuclear magnetic resonance spectroscopy. II. Changes during ischaemia. J Cereb Blood Flow Metab 1987; 7: 394–402.CrossRefGoogle ScholarPubMed
Petroff, OA, Prichard, JW, Ogino, T, Shulman, RG. Proton magnetic resonance spectroscopic studies of agonal carbohydrate metabolism in rabbit brain. Neurology 1988; 38: 1569–1574.CrossRefGoogle ScholarPubMed
Dreher, W, Kuhn, B, Gyngell, ML, et al. Temporal and regional changes during focal ischemia in rat brain studied by proton spectroscopic imaging and quantitative diffusion NMR imaging. Magn Reson Med 1998; 39: 878–888.CrossRefGoogle ScholarPubMed
Norris, DG, Hoehn-Berlage, M, Dreher, W, et al. Characterization of middle cerebral artery occlusion infarct development in the rat using fast nuclear magnetic resonance proton spectroscopic imaging and diffusion-weighted imaging. J Cereb Blood Flow Metab 1998; 18: 749–757.CrossRefGoogle ScholarPubMed
Nagatomo, Y, Wick, M, Prielmeier, F, Frahm, J. Dynamic monitoring of cerebral metabolites during and after transient global ischemia in rats by quantitative proton NMR spectroscopy in vivo. NMR Biomed 1995; 8: 265–270.CrossRefGoogle ScholarPubMed
Rumpel, H, Lim, WE, Chang, HM, et al. Is myo-inositol a measure of glial swelling after stroke? A magnetic resonance study. J Magn Reson Imaging. 2003; 17: 11–19.CrossRefGoogle ScholarPubMed
Felber, SR, Aichner, FT, Sauter, R, Gerstenbrand, F. Combined magnetic resonance imaging and proton magnetic resonance spectroscopy of patients with acute stroke. Stroke 1992; 23: 1106–1110.CrossRefGoogle ScholarPubMed
Gideon, P, Henriksen, O, Sperling, B, et al. Early time course of N-acetylaspartate, creatine and phosphocreatine, and compounds containing choline in the brain after acute stroke. Stroke 1992; 23: 1566–1572.CrossRefGoogle ScholarPubMed
Henriksen, O, Gideon, P, Sperling, B, et al. Cerebral lactate production and blood flow in acute stroke. J Magn Reson Imaging. 1992; 2: 511–517.CrossRefGoogle ScholarPubMed
Fenstermacher, MJ, Narayana, PA. Serial proton magnetic resonance spectroscopy of ischemic brain injury in humans. Invest Radiol 1990; 25: 1034–1039.CrossRefGoogle ScholarPubMed
Gideon, P, Sperling, B, Arlien-Soborg, P, Olsen, TS, Henriksen, O. Long-term follow-up of cerebral infarction patients with proton magnetic resonance spectroscopy. Stroke 1994; 25: 967–973.CrossRefGoogle ScholarPubMed
Sappey-Marinier, D, Calabrese, G, Hetherington, HP, et al. Proton magnetic resonance spectroscopy of human brain: applications to normal white matter, chronic infarction, and MRI white matter signal hyperintensities. Magn Reson Med 1992; 26: 313–327.CrossRefGoogle ScholarPubMed
Graham, GD, Blamire, AM, Howseman, AM, et al. Proton magnetic resonance spectroscopy of cerebral lactate and other metabolites in stroke patients. Stroke 1992; 23: 333–340.CrossRefGoogle ScholarPubMed
Graham, G, Blamire, A, Rothman, D, et al. Early temporal variation of cerebral metabolites after human stroke. Stroke 1993; 24: 1891–1896.CrossRefGoogle ScholarPubMed
Hugg, JW, Duijn, JH, Matson, GB, et al. Elevated lactate and alkalosis in chronic human brain infarction observed by 1H and 31P MR spectroscopic imaging. J Cereb Blood Flow Metab 1992; 12: 734–744.CrossRefGoogle ScholarPubMed
Sorensen, AG, Buonanno, FS, Gonzalez, RG, et al. Hyperacute stroke: evaluation with combined multisection diffusion-weighted and hemodynamically weighted echo-planar MR imaging. Radiology 1996; 199: 391–401.CrossRefGoogle ScholarPubMed
Rutgers, DR, Klijn, CJ, Kappelle, LJ, van der Grond, J. Cerebral metabolic changes in patients with a symptomatic occlusion of the internal carotid artery: a longitudinal 1H magnetic resonance spectroscopy study. J Magn Reson Imaging 2000; 11: 279–286.3.0.CO;2-0>CrossRefGoogle ScholarPubMed
Klijn, CJ, Kappelle, LJ, van der Grond, J, et al. Magnetic resonance techniques for the identification of patients with symptomatic carotid artery occlusion at high risk of cerebral ischemic events. Stroke 2000; 31: 3001–3007.CrossRefGoogle ScholarPubMed
van der Grond, J, Balm, R, Klijn, CJ, et al. Cerebral metabolism of patients with stenosis of the internal carotid artery before and after endarterectomy. J Cereb Blood Flow Metab 1996; 16: 320–326.CrossRefGoogle ScholarPubMed
Pendlebury, ST, Blamire, AM, Lee, MA, Styles, P, Matthews, PM. Axonal injury in the internal capsule correlates with motor impairment after stroke. Stroke 1999; 30: 956–962.CrossRefGoogle ScholarPubMed
De Stefano, N, Narayanan, S, Francis, GS, et al. Evidence of axonal damage in the early stages of multiple sclerosis and its relevance to disability. Arch Neurol 2001; 58: 65–70.CrossRefGoogle ScholarPubMed
Federico, F, Simone, IL, Conte, C, et al. Prognostic significance of metabolic changes detected by proton magnetic resonance spectroscopy in ischaemic stroke. J Neurol 1996; 243: 241–247.CrossRefGoogle ScholarPubMed
Parsons, MW, Li, T, Barber, PA, et al. Combined (1)H MR spectroscopy and diffusion-weighted MRI improves the prediction of stroke outcome. Neurology 2000; 55: 498–505.CrossRefGoogle ScholarPubMed
Pereira, AC, Saunders, DE, Doyle, VL, et al. Measurement of initial N-acetyl aspartate concentration by magnetic resonance spectroscopy and initial infarct volume by MRI predicts outcome in patients with middle cerebral artery territory infarction. Stroke 1999; 30: 1577–1582.CrossRefGoogle ScholarPubMed
Carhuapoma, JR, Wang, PY, Beauchamp, NJ, et al. Diffusion-weighted MRI and proton MR spectroscopic imaging in the study of secondary neuronal injury after intracerebral hemorrhage. Stroke 2000; 31: 726–732.CrossRefGoogle Scholar
Parsons, MW, Barber, PA, Desmond, PM, et al. Acute hyperglycemia adversely affects stroke outcome: a magnetic resonance imaging and spectroscopy study. Ann Neurol 2002; 52: 20–28.CrossRefGoogle ScholarPubMed

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